Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42683273-42683465 | Common:3; Rare:76 | ||||
chr1:42767023-42767309 | Common:4; Rare:88 | ||||
chr1:42817213-42817460 | Rare:92 | ||||
chr1:42846392-42846640 | Common:1; Rare:68 | ||||
chr1:42958862-42958969 | Rare:26; Clinvar:2; Clinvar (benign):1 | ||||
chr1:43358829-43359006 | Rare:45 | ||||
chr1:43367965-43368187 | Rare:59 | ||||
chr1:43389752-43389945 | Common:3; Rare:87 | ||||
chr1:43649869-43650204 | Rare:78 | ||||
chr1:43946626-43946983 | Rare:95 | ||||
chr1:44674421-44674724 | Common:3; Rare:79 | ||||
chr1:44739641-44739889 | Common:2; Rare:97 | ||||
chr1:44775469-44775599 | Rare:53 | ||||
chr1:44775797-44776140 | Common:2; Rare:121 | ||||
chr1:44986532-44986802 | Common:2; Rare:55; Clinvar (benign):1 |